The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Elimination of p19ARF-expressing cells enhances pulmonary function in mice
Open accessAbstract
Senescent cells accumulate in many tissues as animals age and are considered to underlie several aging-associated pathologies. The tumor suppressors p19 ARF and p16 INK4a , both of which are encoded in the CDKN2A locus, play critical roles in inducing and maintaining permanent cell cycle arrest during cellular senescence. Although the elimination of p16 INK4a -expressing cells extends the life span of the mouse, it is unclear whether tissue function is restored by the elimination of senescent cells in aged animals and whether and how p19 ARF contributes to tissue aging. The aging-associated decline in lung function is characterized by an increase in compliance as well as pathogenic susceptibility to pulmonary diseases. We herein demonstrated that pulmonary function in 12-month-old mice was reversibly restored by the elimination of p19 ARF -expressing cells. The ablation of p19 ARF -expressing cells using a toxin receptor-mediated cell knockout system ameliorated aging-associated lung hypofunction. Furthermore, the aging-associated gene expression profile was reversed after the elimination of p19 ARF . Our results indicate that the aging-associated decline in lung function was, at least partly, attributed to p19 ARF and was recovered by eliminating p19 ARF -expressing cells.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Converging evidence suggests that the aging hallmark, cellular senescence, may be a central mechanism contributing to IPF [6,7].”
From Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study (2019) · cites this paper as [7]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Very recently, Hashimoto et al. provided crucial evidence that cellular senescence contributes to lung ageing and may be targeted for functional improvement20.”
From Cellular senescence mediates fibrotic pulmonary disease (2017) · cites this paper as [20]
In the citing paper
“cellular senescence has emerged as the nexus between chronological aging and deficits in the structure and function of multiple organs”
From Skeletal muscle aging, cellular senescence, and senotherapeutics: current knowledge and future directions (2021) · cites this paper as Hashimoto et al., 2016
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
KEGG: Kyoto Encyclopedia of Genes and Genomes
Kanehisa, M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.27 · Cited by 37,077
KEGG: Kyoto Encyclopedia of Genes and Genomes
Ogata, H., Goto, S., Sato, K., Fujibuchi, W., Bono, H., & Kanehisa, M. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.1.29 · Cited by 31,232
The serial cultivation of human diploid cell strains
Hayflick, L., & Moorhead, P. S. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90192-6 · Cited by 8,508
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., & Pereira-Smith, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9363 · Cited by 7,477
The senescence-associated secretory phenotype: the dark side of tumor suppression
Coppé, J.-P., Desprez, P.-Y., Krtolica, A., & Campisi, J. (2010) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-121808-102144 · Cited by 5,206
Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders
Baker, D. J., Wijshake, T., Tchkonia, T., LeBrasseur, N. K., Childs, B. G., van de Sluis, B., Kirkland, J. L., & van Deursen, J. M. (2011) · Nature · doi:10.1038/nature10600 · Cited by 3,670
Data, information, knowledge and principle: back to metabolism in KEGG
Kanehisa, M. I., Goto, S., Sato, Y., Kawashima, M., Furumichi, M., & Tanabe, M. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1076 · Cited by 3,103
Naturally occurring p16Ink4a-positive cells shorten healthy lifespan
Baker, D. J., Childs, B. G., Durik, M., Wijers, M. E., Sieben, C. J., Zhong, J., A. Saltness, R., Jeganathan, K. B., Verzosa, G. C., Pezeshki, A., et al. (2016) · Nature · doi:10.1038/nature16932 · Cited by 2,876
Cellular senescence: from physiology to pathology
Muñoz-Espín, D., & Serrano, M. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3823 · Cited by 2,818
The role of senescent cells in ageing
van Deursen, J. M. (2014) · Nature · doi:10.1038/nature13193 · Cited by 2,623
The Achilles' heel of senescent cells: from transcriptome to senolytic drugs
Zhu, Y., Tchkonia, T., Pirtskhalava, T., Gower, A. C., Ding, H., Giorgadze, N., Palmer, A. K., Ikeno, Y., Hubbard, G. B., Lenburg, M., et al. (2015) · Aging Cell · doi:10.1111/acel.12344 · Cited by 2,584
Cellular senescence in aging and age-related disease: from mechanisms to therapy
Childs, B. G., Durik, M., Baker, D. J., & van Deursen, J. M. (2015) · Nature Medicine · doi:10.1038/nm.4000 · Cited by 2,363
A complex secretory program orchestrated by the inflammasome controls paracrine senescence
Acosta, J. C., Banito, A., Wuestefeld, T., Georgilis, A., Janich, P., Morton, J. P., Athineos, D., Kang, T.-W., Lasitschka, F., Andrulis, M., et al. (2013) · Nature Cell Biology · doi:10.1038/ncb2784 · Cited by 2,278 · cited 6×
“The contribution of senescent cells in aging-associated phenotypes may depend on their non–cellautonomous functions, such as senescence-associated secretory phenotype (SASP), because the population of senescent cells is very small, even in very old human tissue (10).”
BackgroundInfluentialPersistent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion
Rodier, F., Coppé, J.-P., Patil, C. K., Hoeijmakers, W. A. M., Muñoz, D. P., Raza, S. R., Freund, A., Campeau, E., Davalos, A. R., & Campisi, J. (2009) · Nature Cell Biology · doi:10.1038/ncb1909 · Cited by 2,232
An Essential Role for Senescent Cells in Optimal Wound Healing through Secretion of PDGF-AA
Demaria, M., Ohtani, N., Youssef, S. A., Rodier, F., Toussaint, W., Mitchell, J. R., Laberge, R.-M., Vijg, J., Van Steeg, H., Dollé, M. E. T., et al. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.012 · Cited by 2,045
Senescence of Activated Stellate Cells Limits Liver Fibrosis
Krizhanovsky, V., Yon, M., Dickins, R. A., Hearn, S., Simon, J., Miething, C., Yee, H., Zender, L., & Lowe, S. W. (2008) · Cell · doi:10.1016/j.cell.2008.09.015 · Cited by 2,027
Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
Chang, J., Wang, Y., Shao, L., Laberge, R.-M., Demaria, M., Campisi, J., Janakiraman, K., Sharpless, N. E., Ding, S., Feng, W., et al. (2016) · Nature Medicine · doi:10.1038/nm.4010 · Cited by 1,819
Tumor Suppression at the Mouse INK4a Locus Mediated by the Alternative Reading Frame Product p19
Kamijo, T., Zindy, F., Roussel, M. F., Quelle, D. E., Downing, J. R., Ashmun, R. A., Grosveld, G., & Sherr, C. J. (1997) · Cell · doi:10.1016/s0092-8674(00)80452-3 · Cited by 1,566
Ink4a/Arf expression is a biomarker of aging
Krishnamurthy, J., Torrice, C., Ramsey, M. R., Kovalev, G. I., Al-Regaiey, K., Su, L., & Sharpless, N. E. (2004) · Journal of Clinical Investigation · doi:10.1172/jci22475 · Cited by 1,486
Requirement for Macrophage Elastase for Cigarette Smoke-Induced Emphysema in Mice
Hautamaki, R. D., Kobayashi, D. K., Senior, R. M., & Shapiro, S. D. (1997) · Science · doi:10.1126/science.277.5334.2002 · Cited by 1,470
Programmed cell senescence during mammalian embryonic development
Muñoz-Espín, D., Cañamero, M., Maraver, A., Gómez-López, G., Contreras, J., Murillo-Cuesta, S., Rodríguez-Baeza, A., Varela-Nieto, I., Ruberte, J., Collado, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.019 · Cited by 1,428
Inflammatory networks during cellular senescence: causes and consequences.
Freund, A., Orjalo, A. V., Desprez, P.-Y., & Campisi, J. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.03.003 · Cited by 1,354
Myc signaling via the ARF tumor suppressor regulates p53-dependent apoptosis and immortalization
Zindy, F., Eischen, C. M., Randle, D. H., Kamijo, T., Cleveland, J. L., Sherr, C. J., & Roussel, M. F. (1998) · Genes & Development · doi:10.1101/gad.12.15.2424 · Cited by 1,245
Senescence is a developmental mechanism that contributes to embryonic growth and patterning
Storer, M., Mas, A., Robert-Moreno, A., Pecoraro, M., Ortells, M. C., Di Giacomo, V., Yosef, R., Pilpel, N., Krizhanovsky, V., Sharpe, J., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.041 · Cited by 1,186
The signals and pathways activating cellular senescence
Ben-Porath, I., & Weinberg, R. A. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.10.013 · Cited by 1,046
Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis
Sharpless, N. E., Bardeesy, N., Lee, K.-H., Carrasco, D., Castrillon, D. H., Aguirre, A. J., Wu, E. A., Horner, J. W., & DePinho, R. A. (2001) · Nature · doi:10.1038/35092592 · Cited by 848
Biological role of matrix metalloproteinases: a critical balance
Löffek, S., Schilling, O., & Franzke, C.-W. (2010) · European Respiratory Journal · doi:10.1183/09031936.00146510 · Cited by 796
Divorcing ARF and p53: an unsettled case
Sherr, C. J. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1954 · Cited by 595
Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice
Krimpenfort, P., Quon, K. C., Mooi, W. J., Loonstra, A., & Berns, A. (2001) · Nature · doi:10.1038/35092584 · Cited by 568 · cited 10×
“Embryonic fibroblasts prepared from these mice (MEFs) expressed p19ARF, p16INK4a, p21, and luciferase when senescence was induced by either serial passages or oncogenic Ras (Figure 1, B and C).”
BackgroundInfluentialDiphtheria toxin receptor–mediated conditional and targeted cell ablation in transgenic mice
Saito, M., Iwawaki, T., Taya, C., Yonekawa, H., Noda, M., Inui, Y., Mekada, E., Kimata, Y., Tsuru, A., & Kohno, K. (2001) · Nature Biotechnology · doi:10.1038/90795 · Cited by 512
An epithelial circadian clock controls pulmonary inflammation and glucocorticoid action
Gibbs, J. E., Ince, L. M., Matthews, L. C., Mei, J., Bell, T., Yang, N., Saer, B., Begley, N., Poolman, T. M., Pariollaud, M., et al. (2014) · Nature Medicine · doi:10.1038/nm.3599 · Cited by 464
Murphy, G., Cockett, M. I., Ward, R. V., & Docherty, A. (1991) · Biochemical Journal · doi:10.1042/bj2770277 · Cited by 457
Coppé, J.-P., Patil, C. K., Rodier, F., Krtolica, A., Beauséjour, C. M., Parrinello, S., Hodgson, J. G., Chin, K., Desprez, P.-Y., & Campisi, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009188 · Cited by 455
Dimri, G. P., Itahana, K., Acosta, M., & Campisi, J. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.1.273-285.2000 · Cited by 401
Evidence of an epithelial stem/progenitor cell hierarchy in the adult mouse lung
McQualter, J. L., Yuen, K., Williams, B., & Bertoncello, I. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909207107 · Cited by 386
Cigarette smoke induces cellular senescence
Nyunoya, T., Monick, M. M., Klingelhutz, A., Yarovinsky, T. O., Cagley, J. R., & Hunninghake, G. W. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0169oc · Cited by 306
Verbeken, E. K., Cauberghs, M., Mertens, I., Clement, J., Lauweryns, J. M., & Van de Woestijne, K. P. (1992) · Chest · doi:10.1378/chest.101.3.793 · Cited by 289
Knudsen, L., Weibel, E. R., Gundersen, H. J. G., Weinstein, F. V., & Ochs, M. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01100.2009 · Cited by 281
Circadian rhythm reprogramming during lung inflammation
Haspel, J. A., Chettimada, S., Shaik, R. S., Chu, J., Raby, B. A., Cernadas, M., Carey, V. J., Process, V., Hunninghake, G. M., Ifedigbo, E., et al. (2014) · Nature Communications · doi:10.1038/ncomms5753 · Cited by 263
Cigarette Smoke Induces Senescence in Alveolar Epithelial Cells
Tsuji, T., Aoshiba, K., & Nagai, A. (2004) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2003-0290oc · Cited by 251
Clinical strategies and animal models for developing senolytic agents
Kirkland, J. L., & Tchkonia, T. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2014.10.012 · Cited by 168
Chronic Obstructive Pulmonary Disease: Risk Factors, Pathophysiology and Pathogenesis
Snider, G. L. (1989) · Annual Review of Medicine · doi:10.1146/annurev.me.40.020189.002211 · Cited by 168
Point mutation of bacterial artificial chromosomes by ET recombination
Muyrers, J. P. P., Zhang, Y., Beneš, V., Testa, G., Ansorge, W. J., & Stewart, A. F. (2000) · EMBO Reports · doi:10.1093/embo-reports/kvd049 · Cited by 134
The effect of age on lung structure in male BALB/cNNia inbred mice
Kawakami, M., Paul, J. L., & Thurlbeck, W. M. (1984) · American Journal of Anatomy · doi:10.1002/aja.1001700102 · Cited by 119
Shalaby, K. H., Gold, L., Schuessler, T. F., Martin, J. G., & Robichaud, A. (2010) · Respiratory Research · doi:10.1186/1465-9921-11-82 · Cited by 116
Verbeken, E. K., Cauberghs, M., Mertens, I., Clement, J., Lauweryns, J. M., & Van de Woestijne, K. P. (1992) · Chest · doi:10.1378/chest.101.3.800 · Cited by 112
Age-dependent changes of airway and lung parenchyma in C57BL/6J mice
Huang, K., Rabold, R., Schofield, B., Mitzner, W., & Tankersley, C. G. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00400.2006 · Cited by 102
McDougall, J. J., Bray, R. C., & Sharkey, K. A. (1997) · The Anatomical Record · doi:10.1002/(sici)1097-0185(199705)248:1 · Cited by 97
A Carbon Nanotube Toxicity Paradigm Driven by Mast Cells and the IL‐33/ST2 Axis
Katwa, P., Wang, X., Urankar, R. N., Podila, R., Hilderbrand, S. C., Fick, R. B., Rao, A. M., Ke, P. C., Wingard, C. J., & Brown, J. M. (2012) · Small · doi:10.1002/smll.201200873 · Cited by 97
Ablation of the p16INK4a tumour suppressor reverses ageing phenotypes of klotho mice
Sato, S., Kawamata, Y., Takahashi, A., Imai, Y., Hanyu, A., Okuma, A., Takasugi, M., Yamakoshi, K., Sorimachi, H., Kanda, H., et al. (2015) · Nature Communications · doi:10.1038/ncomms8035 · Cited by 77
Inflammaging increases susceptibility to cigarette smoke-induced COPD
John-Schuster, G., Günter, S., Hager, K., Conlon, T. M., Eickelberg, O., & Yildirim, A. Ö. (2015) · Oncotarget · doi:10.18632/oncotarget.4027 · Cited by 59
Yamamoto, Y., Tanaka, A., Kanamaru, A., Tanaka, S., Tsubone, H., Atoji, Y., & Suzuki, Y. (2003) · The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology · doi:10.1002/ar.a.10172 · Cited by 41
Churchman, M. L., Roig, I., Jasin, M., Keeney, S., & Sherr, C. J. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002157 · Cited by 35
Abe, K., Hazama, M., KATOH, H., Yamamura, K., & Suzuki, M. (2004) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.53.311 · Cited by 32
Chronic Cigarette Smoke Inhalation and Aging in Mice
Matulionis, D. H. (1984) · Experimental Lung Research · doi:10.3109/01902148409087916 · Cited by 32
A Diphtheria Toxin Receptor Deficient in Epidermal Growth Factor–Like Biological Activity
Furukawa, N., Saito, M., Hakoshima, T., & Kohno, K. (2006) · The Journal of Biochemistry · doi:10.1093/jb/mvj216 · Cited by 31
Mechanical interdependence in relation to age: effects of lung volume on airway resistance in rats
Nagase, T., Fukuchi, Y., Teramoto, S., Matsuse, T., & Orimo, H. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.3.1172 · Cited by 31
Age-related changes in the static and dynamic mechanical properties of mouse lungs
Hirai, T., Hosokawa, M., Kawakami, K., Takubo, Y., Sakai, N., Oku, Y., Chin, K., Ohi, M., Higuchi, K., Kuno, K., et al. (1995) · Respiration Physiology · doi:10.1016/0034-5687(95)00068-2 · Cited by 24
E2F-Dependent Induction of p14ARF During Cell Cycle Re-entry in Human T Cells
del Arroyo, A. G., Messaoudi, S. E., Clark, P. A., James, M. C., Stott, F. J., Bracken, A. P., Helin, K., & Peters, G. G. (2007) · Cell Cycle · doi:10.4161/cc.6.21.4857 · Cited by 24
HuR Maintains a Replicative Life Span by Repressing the ARF Tumor Suppressor
Kawagishi, H., Hashimoto, M., Nakamura, H., Tsugawa, T., Watanabe, A., Kontoyiannis, D. L., & Sugimoto, M. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.01277-12 · Cited by 15
Self-citation
Flagged first, then by citations
Research works printed but not linked: 1
- 10.1016/j.cell.2008.06.049 · DOI · Paper page
Cited by
Sorted by citations
Mechanisms of Cellular Senescence: Cell Cycle Arrest and Senescence Associated Secretory Phenotype
Kumari, R., & Jat, P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.645593 · Cited by 1,622
Cellular senescence mediates fibrotic pulmonary disease
Schafer, M. J., White, T. A., Iijima, K., Haak, A. J., Ligresti, G., Atkinson, E. J., Oberg, A. L., Birch, J., Salmonowicz, H., Zhu, Y., et al. (2017) · Nature Communications · doi:10.1038/ncomms14532 · Cited by 1,613
“Attenuation of age-related pathologies and extension of lifespan in chronologically aged mice has been demonstrated using the same transgenic strategy 32–34 , and improvements in lung structure and function in aged mice have recently been demonstrated using a similar suicide-gene strategy 20 .”
Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study
Justice, J. N., Nambiar, A. M., Tchkonia, T., LeBrasseur, N. K., Pascual, R., Hashmi, S. K., Prata, L., Masternak, M. M., Kritchevsky, S. B., Musi, N., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2018.12.052 · Cited by 1,261
Senescent cell clearance by the immune system: Emerging therapeutic opportunities
Prata, L. G. P. L., Ovsyannikova, I. G., Tchkonia, T., & Kirkland, J. L. (2018) · Seminars in Immunology · doi:10.1016/j.smim.2019.04.003 · Cited by 497
Stress, cell senescence and organismal ageing
de Magalhães, J. P., & Passos, J. F. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.07.001 · Cited by 316
Metadata
- Authors
- Hashimoto, M., Asai, A., Kawagishi, H., Mikawa, R., Iwashita, Y., Kanayama, K., Sugimoto, K., Sato, T., Maruyama, M., & Sugimoto, M.
- Affiliations
- National Center for Geriatrics and Gerontology (JP)
- Department of Oncologic Pathology and
- Mie University (JP)
- Juntendo University (JP)
- Corresponding author
- Sugimoto, Masataka
- ORCID
- Venue
- JCI Insight
- Published
- 2016-08-04
- Volume
- 1
- Issue
- 12
- Pages
- e87732-e87732
- ISSN
- 2379-3708 (ISSN-L)
- PMC
- PMC5033852
- OpenAlex
- W2497953377
- Semantic Scholar
- 09c297e32bfdab931b8cfc06cdce69f1fe3aea3e
- Cited by
- 162
- References
- 60
- Citations by year
- 2026: 10 · 2025: 11 · 2024: 15 · 2023: 16 · 2022: 12 · 2021: 23 · 2020: 20 · 2019: 21 · 2018: 19 · 2017: 15
- FWCI
- 14.76
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- JCI Insight (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Aichi Health Promotion Foundation
- National Center for Geriatrics and Gerontology (28-22)
- Japan Foundation for Aging and Health
- Japan Society for the Promotion of Science (26461199, 16K08604)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- cellular senescence, p19ARF, p16INK4a, CDKN2A, senolytics, senescent cell elimination, lung aging, lung function, lung compliance, tissue aging
- MeSH terms
- Aging, Animals, Lung, Mice, Inbred C57BL, Mice, Transgenic, Respiratory Function Tests, Cellular Senescence, Tumor Suppressor Protein p14ARF, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review